Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516165
rs397516165
MYH7
T 0.700 GeneticVariation CLINVAR Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257

2017
dbSNP: rs397516165
rs397516165
MYH7
T 0.700 GeneticVariation CLINVAR Loss of Function Mutations in NNT Are Associated With Left Ventricular Noncompaction. 26025024

2015
dbSNP: rs397516165
rs397516165
MYH7
T 0.700 GeneticVariation CLINVAR Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians. 25448463

2014
dbSNP: rs397516165
rs397516165
MYH7
T 0.700 GeneticVariation CLINVAR Electrocardiographic features of sarcomere mutation carriers with and without clinically overt hypertrophic cardiomyopathy. 21943931

2011
dbSNP: rs397516165
rs397516165
MYH7
T 0.700 GeneticVariation CLINVAR Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart Failure. 21750094

2011